J4 ›› 2012, Vol. 25 ›› Issue (1): 103-107.doi: 10.3976/j.issn.1002-4026.2012.01.022

• 目录 • 上一篇    下一篇

超分子包合技术在新药研制中的应用

赵梅,王晓东,王晓,张莉莉,李恩霞   

  1. 山东省分析测试中心,山东 济南 250014
  • 收稿日期:2011-09-05 出版日期:2012-02-20 发布日期:2012-02-20
  • 作者简介:赵梅(1981-),女,硕士研究生,研究方向为超分子化学。Email:chzhaomei@yahoo.cn

Application of supramolecular inclusion technique in pharmaceutical development

 ZHAO Mei, WANG Xiao-Dong, WANG Xiao, ZHANG Li-Li, LI En-Xia   

  1. Shandong Analysis and Test Center, Jinan 250014, China
  • Received:2011-09-05 Online:2012-02-20 Published:2012-02-20

摘要:

        在药物研究中用以进行超分子包合研究的主体有冠醚、环糊精、杯芳烃及瓜环等,它们均具有穴状结构,能通过非共价键与离子及中性分子形成超分子,可以提高药物的稳定性。本文重点介绍了这几种主要的超分子包合主体在药物研发中的应用研究进展,并对超分子包合技术在新药研制中的应用前景进行了展望。

关键词: 超分子包合技术, 包合作用, 药物研制, 包合物

Abstract:

        In pharmaceutical research,the supramolecular inclusion hosts include crown ether, cyclodextrin, calixarene and cucurbituril. They all have cavity structure and can form supermolecules with other ions and neutral molecules by the noncovalent bonds,which can improve medical stability. This paper surveys application advances of these supramolecular hosts in the pharmaceutical development.It also presents the application prospect of supramolecular inclusion technique in new medicine development.

Key words: supramolecular inclusion technique, inclusion effect, pharmaceutical development, inclusion compound

中图分类号: 

  • TQ460.6